Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3035975016 | Genetic leukocyte disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
3036234010 | Genetic leucocyte disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
494971014 | Genetic anomaly of leucocyte | en | Synonym | Active | Case insensitive | SNOMED CT core |
785504010 | Genetic anomaly of leukocyte (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
79970019 | Genetic anomaly of leukocyte | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Pelger-Huët anomaly | Is a | True | Genetic anomaly of leucocyte | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set